Canonical Allele Identifier: CA2681000583

Gene: RSPH3

Linked Data

• gnomAD v4: 6-158982436-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158982436G>A , CM000668.2:g.158982436G>A	GRCh38
NC_000006.11:g.159403468G>A , CM000668.1:g.159403468G>A	GRCh37
NC_000006.10:g.159323456G>A	NCBI36
NG_051819.1:g.22752C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367069.7:c.696+49C>T MANE Select	ENSP00000356036.1:n.696+49C>T
ENST00000252655.1:c.1122+49C>T	ENSP00000252655.1:n.1122+49C>T
ENST00000367069.6:c.696+49C>T	ENSP00000356036.1:n.696+49C>T
ENST00000449822.5:c.408+49C>T	ENSP00000393195.1:n.408+49C>T
NM_031924.4:c.1122+49C>T	NP_114130.3:n.1122+49C>T
XM_005267153.3:c.834+49C>T	XP_005267210.1:n.834+49C>T
XR_245553.2:n.1578+49C>T
NM_001346418.1:c.834+49C>T	NP_001333347.1:n.834+49C>T
NM_031924.5:c.1122+49C>T	NP_114130.3:n.1122+49C>T
NR_144434.1:n.1333+49C>T
XM_017011347.2:c.306+49C>T	XP_016866836.1:n.306+49C>T
XM_024446566.1:c.306+49C>T	XP_024302334.1:n.306+49C>T
XR_001743668.2:n.1572+49C>T
XR_001743669.2:n.1572+49C>T
XR_001743670.2:n.1284+49C>T
XR_001743671.2:n.778+49C>T
NM_031924.6:c.1122+49C>T	NP_114130.3:n.1122+49C>T
NM_031924.8:c.696+49C>T MANE Select	NP_114130.4:n.696+49C>T